The renin-angiotensin-system and left ventricular mass in young adults: the African-PREDICT study. (4th March 2021)

• Record Type: Journal Article
• Authors: du Toit, Wessel L.; Schutte, Aletta E.; Gafane-Matemane, Lebo F.; Kruger, Ruan; Mels, Catharina M. C.
• Is Part Of: Blood pressure. Volume 30:Number 2(2021)
• Page Start: 98
• Page End: 107
• Publication Date: 2021-03-04
• Subjects: Ethnicity -- left ventricular mass -- renin-angiotensin system -- sex -- socio-economic status; Blood pressure -- Periodicals; Hypertension -- Periodicals; Hypertension -- Periodicals; Blood Pressure -- Periodicals; 612.14
• DOI: 10.1080/08037051.2020.1831902
• Languages: English
• ISSNs: 0803-7051

Abstract

Abstract: Purpose: Raised blood pressure, with the renin-angiotensin system (RAS) as a central regulatory component, is one of the most important contributors to early development of left ventricular hypertrophy. Factors such as increased age, sex, black ethnicity and a low socio-economic status also contribute to left ventricular remodelling. To better understand early contributors to left ventricular mass, we investigated the relationship between left ventricular mass index (LVMi) and the components of the RAS in young healthy adults while considering ethnicity, sex and socio-economic status. Materials and methods: Black and white women and men ( N = 1186) between the ages of 20–30 years were included. By using standard echocardiography, we determined LVMi. Ultra-pressure-liquid chromatography tandem-mass spectrometry (LC-MS/MS) was used to measure the RAS-fingerprint ® . Results: Components of the RAS such as plasma renin activity (PRA-S), angiotensin I (Ang I), angiotensin II (Ang II) and aldosterone were suppressed in the black compared to the white group (all p < 0.001). No associations between LVMi and the RAS were evident in the total, black or white groups. With additional grouping according to sex and socio-economic status, inverse associations between LVMi and PRA-S ( β = −0.168; p = 0.017), Ang I ( β = −0.155; p = 0.028) and Ang II ( β = −0.172; p = 0.015) were found only in low socio-economic black women. Conclusion: Despite a suppressed RAS in the black compared to the white group, components of the RAS were not associated with LVMi in this young cohort. The low socio-economic black women of this study population may be vulnerable to future RAS-related increases in left ventricular mass.